A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv503n106



Internal ID19018612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97275106..97277658hg38UCSC Ensembl
chr10:99034863..99037415hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382553
hg192553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111459, nsv1131849, nsv1130299
SamplesKWS1, KWS2
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv503n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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